Allele Registry

Canonical Allele Identifier: PA239139

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000243232

ClinVar Variation:

193596

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Ser494Asn	CA239138 NM_000500.9:c.1481G>A